Evidence map›Paper›PMID 36941675›Full record

ArticleBMC biology2023

Weak gene-gene interaction facilitates the evolution of gene expression plasticity.

Hao-Chih Kuo, Cheng-Te Yao, Ben-Yang Liao, Meng-Pin Weng, Feng Dong, Yu-Cheng Hsu, Chih-Ming Hung

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In one paragraph

Article in BMC biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Hao-Chih KuoBiodiversity Research Center, Academia Sinica, Taipei, 11529, Taiwan.
Cheng-Te YaoDivision of Zoology, Endemic Species Research Institute, Nantou, 55244, Taiwan.
Ben-Yang LiaoInstitute of Population Health Sciences, National Health Research Institutes, Miaoli, 35053, Taiwan.
Meng-Pin WengInstitute of Population Health Sciences, National Health Research Institutes, Miaoli, 35053, Taiwan.
Feng DongKunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650223, Yunnan, China.
Yu-Cheng HsuDepartment of Natural Resources and Environmental Studies, National Dong Hwa University, Hualien, 97401, Taiwan.
Chih-Ming HungBiodiversity Research Center, Academia Sinica, Taipei, 11529, Taiwan. cmhung@gate.sinica.edu.tw.ORCID 0000-0002-4785-6370
Biodiversity Research Center, Academia Sinica · TWNational Health Research Institutes · TWKunming Institute of Zoology · CNNational Dong Hwa University · TWTaiwan Forestry Research Institute · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndividual organisms may exhibit phenotypic plasticity when they acclimate to different conditions. Such plastic responses may facilitate or constrain the adaptation of their descendant populations to new environments, complicating their evolutionary trajectories beyond the genetic blueprint. Intriguingly, phenotypic plasticity itself can evolve in terms of its direction and magnitude during adaptation. However, we know little about what determines the evolution of phenotypic plasticity, including gene expression plasticity. Recent laboratory-based studies suggest dominance of reversing gene expression plasticity-plastic responses that move the levels of gene expression away from the new optima. Nevertheless, evidence from natural populations is still limited.

resultsHere, we studied gene expression plasticity and its evolution in the montane and lowland populations of an elevationally widespread songbird-the Rufous-capped Babbler (Cyanoderma ruficeps)-with reciprocal transplant experiments and transcriptomic analyses; we set common gardens at altitudes close to these populations' native ranges. We confirmed the prevalence of reversing plasticity in genes associated with altitudinal adaptation. Interestingly, we found a positive relationship between magnitude and degree of evolution in gene expression plasticity, which was pertinent to not only adaptation-associated genes but also the whole transcriptomes from multiple tissues. Furthermore, we revealed that genes with weaker expressional interactions with other genes tended to exhibit stronger plasticity and higher degree of plasticity evolution, which explains the positive magnitude-evolution relationship.

conclusionsOur experimental evidence demonstrates that species may initiate their adaptation to new habitats with genes exhibiting strong expression plasticity. We also highlight the role of expression interdependence among genes in regulating the magnitude and evolution of expression plasticity. This study illuminates how the evolution of phenotypic plasticity in gene expression facilitates the adaptation of species to challenging environments in nature.

Indexed as

AcclimatizationAdaptation, PhysiologicalAltitudeBiological EvolutionGene ExpressionPhenotypeCo-expression connectivityGene expression plasticityHigh-altitude adaptationReciprocal transplant experimentsRNA sequencing

Identifiers

PMID36941675
PMCPMC10029303
OpenAlexW4328049112

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Textfull text, public
LicenceCC BY
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table measurements read30
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None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.